2005, NucleaRDB.
This data was extracted from Medline abstracts and full texts (when available) in an automated manner.
The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation P12A was found are listed after the table.
The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.
| Point mutation: | P12A | |
| Domain: | N-term | |
| General numbering (NucleaRDB): | - | |
| Protein: | PPAT_HUMAN (PPARG,NR1C) | Swiss-Prot Cross-reference table Family page |
| Protein isoforms | 2 | |
| Other point mutations / same protein / same position | Point mutations at position 12 in PPAT_HUMAN | |
| Other point mutations / same protein | List of mutations in PPAT_HUMAN | |
| Family alignments |
1C3 PPAR gamma 1C Peroxisome proliferator activated (PPAR) 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR | |
| Other point mutations / same position | ||
| Reference: | Combined effects of PPARgamma2 P12A and PPARalpha L162V polymorphisms on glucose and insulin homeostasis: the Quebec Family Study. Bosse Y, Weisnagel SJ, Bouchard C, Despres JP, Perusse L, Vohl MC J Hum Genet 2003;48(12):614-21. Epub 2003 Nov 20. | Medline |
| Other point mutations / same article | List | |
| Text source | abstract | |
| Validation status | True positive |
Relevant sentences:
P12A
cmbi.kun.nl), 21-Apr-2005